Steerable ablation device

ABSTRACT

The invention relates to a flexible assembly for use in a region of a medical or surgical device. In preferred embodiments, the flexible region comprises a set of pull wires for controllably moving a treatment end of the device, and elements to separate the pull wires and maintain the integrity of the shaft of the flexible region in order to improve the operating aspects of the device. The devices and methods can be especially useful in ablation treatments, such as ablation at cardiac or epicardial tissues.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.13/873,348, filed 30 Apr. 2013 (the '348 application), now ______; whichis a continuation of U.S. application Ser. No. 11/647,315, filed 29 Dec.2006 (the '315 application), now U.S. Pat. No. 8,444,637. The '348application and '315 application are each incorporated by reference asfully set forth herein.

BACKGROUND OF THE INVENTION

a. Field of the Invention

The instant invention relates to ablation devices, methods of usingthem, and steerable devices for use in medical treatments. Inparticular, the invention relates to devices used in conjunction withatrial fibrillation procedures and improvements related to theintroduction of devices around the heart or at epicardial surfaces.

b. Background Art

A number of surgical procedures employ the use of steerable devices,such as catheters. In an atrial fibrillation treatment for ablatingcardiac tissues, an alternative to the surgical incisions of the heartis the maze procedure, where transmural ablations of the heart are madewithin an ablation device. Such ablations may be performed either fromwithin the chambers of the heart (endocardial ablation) usingendovascular devices (e.g., catheters) introduced through arteries orveins, or from outside the heart (epicardial ablation) using devicesintroduced into the chest. Various ablation techniques have been used,including cryogenic, radiofrequency (RF), laser and microwave, to createelongated transmural lesions and block electrical conduction in theatrial myocardium. An advantageous use of transmural ablation ratherthan surgical incisions is the ability to perform the procedure on thebeating heart without the use of cardiopulmonary bypass. Maintaining theproper positioning against the wall of a beating heart can also bedifficult. Visualization of endocardial anatomy and endovascular devicesis often inadequate and knowing the precise position of such devices inthe heart can be difficult, resulting in misplaced lesions.

Epicardial ablation devices and methods useful for creating transmurallesions for the treatment of atrial fibrillation have been described inU.S. Pat. No. 7,052,493 to Vaska et al. (“Vaska”) and U.S. Pat. No.6,971,394 to Sliwa et al. (“Sliwa”), both of which are hereby expresslyincorporated by reference. Sliwa describes a method of forming atransmural lesion in a wall of the heart adjacent to the pulmonary veinsby placing an ablation device through a thoracic incision and thenthrough a pericardial penetration so that the ablation device isdisposed in contact with an epicardial surface of the heart. Vaskadescribes an ablation device and system which may be used to wrap anablation device around the pulmonary veins at an epicardial location.

Execution of a contiguous pulmonary vein (PV) isolation procedure canoccasionally present considerable challenges to the physician.Difficulties in maneuvering the devices and passing them aroundanatomical structures, maintaining accurate placement on a beatingheart, and avoiding unintended contact with other tissues mean that ahigh degree of physician skill and experience may be required in somecircumstances. What are needed, therefore, are devices and methods whichallow for precise introduction and placement of the ablation elements inPV isolation and linear left atrial ablations. More particularly,devices and methods which insure that ablation devices are properlyplaced or introduced for a PV isolation or mitral isthmus ablationprocedure are desired.

BRIEF SUMMARY OF THE INVENTION

It is desirable to be able to maneuver or steer an ablation cell ordevice near epicardial surfaces and other areas in surgical procedureswithout concern for the unintended movement or reaction of the devicewhile in the body. The invention relates to a flexible assembly for usein a region of a medical or surgical device. In preferred embodiments,the flexible region comprises a set of pull wires for controllablymoving a treatment end of the device, and elements to separate the pullwires and maintain the integrity of the shaft of the flexible region inorder to improve the operating aspects of the device. The devices andmethods can be especially useful in ablation treatments, such asablation at cardiac or epicardial tissues.

The present invention meets these and other objectives by providingdevices, assemblies, and methods for placing and controlling themovement of medical devices. For example, some steerable devices maycrimp or twist if deflected too far or deflected suddenly or forcefully.In addition, some flexible device may break if deflected too far. Theinvention provides a medical device, such as a catheter or shaft forintroduction into the body or an assembly therefor, having improvedstructural properties and steerable characteristics that, in part,addresses these shortcomings in some existing devices. In particular andin one aspect, the invention provides a steerable wand or shaft-typedevice, or assembly therefor, for controllably introducing and/orpositioning an ablation element on a cardiac or epicardial surface.However, the invention is not limited to use in cardiac procedures orwith ablation treatments or devices. Instead, the invention relates moregenerally to deflectable or steerable medical devices that contain aflexible support region that allows a desired degree of deflection andprevents crimping, breaking, twisting or other movements that may effectthe controllability of the device.

Thus, in one aspect, the invention includes an assembly for a steerabledevice for use in surgical or ablation therapy wherein the devicetypically has an elongated shaft with a flexible distal region and agenerally straight proximal region. In the example of an ablatingdevice, one or more ablation elements or cells are disposed along thedistal end of the device, but which need not be part of the assemblyitself. A steerable deflection area is defined within the flexibleregion, and it includes a first anchor member, preferably a ring-shapedor other shape to accommodate the profile associated with the shaft ofthe device, attached to a distal portion of the flexible distal region.The anchor member has one or more passageways for one or more pull wiresextending from the proximal region and one or more actuators to thedistal region. The steerable deflection region comprises a coiled orinterlocking flex support member designed to permit deflection to adesired angle of deflection and maintain the integrity of the interiorand exterior of the device during its use in a procedure. Typically, theproximal region of the elongated shaft contains one or more actuators tocontrol the movement of the steerable deflection region, such that, forexample, the distal region and distal end of the device move in responseto actuation of the one or more pull wires.

The invention also includes methods to design and produce flexibleassemblies to allow a desired range of controlled motion for a distalend of a device. For example, if the desired range of deflection of thedistal end is from a straight to a 60 degree angle, the flexible supportmember, its structure and composition, can be selected to substantiallyprevent the flexible region from crimping, yielding, cracking, on itsinterior or exterior surfaces, and/or substantially prevent blocking orinterfering with the movement of pull wires, or twisting or moving inunintended directions or degrees. Thus, the distal end comprising atreatment or diagnostic element can be steered or moved morecontrollably by a physician using the medical device.

A particularly preferred embodiment of the invention includes steerableablation devices having a shaft with a flexible distal region and agenerally straight proximal region. One or more ablation cells aredisposed along the distal end, which has a steerable deflection degreedefined be a region of the device assembly within a designed flexibleregion. The steerable deflection region has at least one anchor memberattached to a distal portion of the flexible distal region, the anchormember having passageways for one or more pull wires extending from theproximal region to the distal region. The steerable deflection regioncomprises a coiled or interlocking flex support member designed topermit deflection to a desired angle of deflection or range ofdeflection angles, and at the same time maintain the integrity of theinterior and/or exterior of the steerable deflection region to preventunintended movement, or prevent during multiple maximum deflections andrelaxations of the device cracking, breaking, crimping, or yielding inthe flexible region. Thus, in particularly preferred embodiments, theinterlocking flex support member can be a laser cut metal or polymerformed into a ribbed-like coil, such as those shown in the figures,which maintains the integrity of the flexible region by substantiallypreventing breaking, cracking, yielding, or crimping of the flexibleregion over the course of 10 or 20 or 50 maximum deflection andrelaxation cycles of the flexible region, for example. The steerabledevice can have two or more pull wires for deflection of the distal endin at least two directions. In preferred embodiments, the flexibleregion includes a flexible separating member within the steerabledeflection region, where the flexible separating member is disposed inthe flexible distal region to maintain the pull wires on separate sidesof the interior of the flexible distal region. As described herein, thecoiled or interlocking flex support member can be comprised of one ormore of a polymer, metal, nitinol, or combination of two or more ofthese materials. The selection of the material and shape of the coiledor interlocking support member can include pre-formed linear, curved, orcurvilinear shapes, for example. The steerable device typically has oneor more pull wires actuated by a handle at the proximal end of thedevice.

The invention also includes methods of using a steerable device of theinvention, such as introducing the flexible distal region and distal endof the device into a body during a surgical treatment and moving thedistal end through actuating at least one pull wire. Preferred methodsinclude those where the surgical procedure comprises ablation of cardiacor pericardial tissue, or where the ablation comprises the use of atleast one ultrasound ablation element.

The foregoing and other aspects, features, details, utilities, andadvantages of the present invention will be apparent from reading thefollowing description and claims, and from reviewing the accompanyingdrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the flexible distal region of a device of the invention.

FIG. 2 depicts an embodiment of the coiled or interlocking supportmember of the flexible distal region.

FIG. 3 depicts an alternate embodiment of the coiled or interlockingsupport member of the flexible distal region.

FIG. 4 depicts an exploded view of exemplary components in a flexibledistal region of a device of the invention.

FIGS. 5 and 6 depict two views of an exemplary anchor member for use inthe invention.

FIG. 7 depicts an exemplary connection area for the anchor member.

FIGS. 8 and 9 depict two additional embodiments of the coiled orinterlocking support member of the flexible distal region.

FIGS. 10 A-C schematically depict the profile shapes of some designs forlaser cut embodiments of an interlocking support member.

DETAILED DESCRIPTION OF THE INVENTION

The headings (such as “Brief Summary”) used are intended only forgeneral organization of topics within the disclosure of the inventionand are not intended to limit the disclosure of the invention or anyaspect of it. In particular, subject matter disclosed in the “BackgroundArt” may include aspects of technology within the scope of the inventionand thus may not constitute solely background to the invention. Subjectmatter disclosed in the “Brief Summary” is not an exhaustive or completedisclosure of the entire scope of the invention or any particularembodiment.

As used herein, the words “preferred,” “preferentially,” and“preferably” refer to embodiments of the invention that afford certainbenefits, under certain circumstances. However, other embodiments mayalso be preferred, under the same or other circumstances. Furthermore,the recitation of one or more preferred embodiments does not imply thatother embodiments are not useful and is not intended to exclude otherembodiments from the scope of the invention and no disclaimer of otherembodiments should be inferred from the discussion of a preferredembodiment or a figure showing a preferred embodiment.

FIGS. 1 and 4 depict different views of a preferred embodiment of theinvention comprising a flexible distal region 5 of a medical device.This assembly can be incorporated into a catheter, ablation device, orother diagnostic or treatment device and function to more controllablyallow the movement of the distal end of the device in response to thephysician's actions on a proximal control or actuating end or handle(not shown). Various deflectable medical devices are known and can bemade available for adaptation with the present invention, includingthose of U.S. published patent applications 20050187455 and 20040034348,and U.S. Pat. Nos. 7,052,493 and 6,971,394, each specificallyincorporated herein by reference. The device can have a pre-formed curveor curvilinear distal region or distal end for use in particularsurgical procedures.

FIG. 1 shows an exemplary assembly with flexible region 5 composed ininterlocking ribbed structure in a flexible support member 3, which canbe any of a number of biocompatible metals, polymers, nitinol,shape-memory polymers or metals, or combinations thereof. In practice,the design of the interlocking ribbed structure should account fordesired degree of deflection for a particular use. For example,interlocking pointed ends in the coiled or interlocking member 3, asshown in FIGS. 1 and 2, allow for a certain degree of movement beforethey become prone to crimping or separating. Similar interlocking ribbedstructures with balled tips, flattened tips, or alternating tips mayallow a greater degree of bending and may be desired for certain uses.FIGS. 10A-C show exemplary laser-cut designs for interlocking ribbedstructures that can provide structural support and maintain theintegrity of the flexible region during maximum deflection. The designsshown in FIGS. 10A-C correspond to a junction point similar to thatshown in FIG. 3, where the points of each of the ribbed coils meet orcome together. These structures can be formed by methods known in theart for laser cutting or other computer numerical control millingmachines, for example. Alternatively, the interlocking area can bedesigned so that the two sides interlock when bent to a certain degree,and then can be held in place at that angle or substantially that angleuntil the area is bent further to release the interlocking A number ofgeometrical shapes and designs can be incorporated into the interlockingarea or ribbed area of the flexible support member. As shown in FIGS. 8and 9, the assembly can include a designed orientation of the ribbedstructure in relation to the direction of deflection allowed in themedical device.

FIG. 3 depicts an alternative coiled structure for this member 3, whichcan similarly be made or comprised of metals, polymers, nitinolshape-memory materials. A variety of spring-like structures, braidedstructures, or coil structures can similarly be used to add structuralintegrity to the flexible distal region of a device according to theinvention.

FIG. 1 further depicts the arrangement of elements in an exemplaryassembly 5. Anchor member 1, here in shape of an anchor ring of the samediameter as the shaft of the device, fits into the distal end 6 of thedistal flexible region of assembly. In this embodiment, a single anchorring is used. The proximal end of the assembly 4 connects to anelongated shaft and optionally terminates in a proximal end handle andactuating elements (not shown). The exterior of the assembly and devicecan be coated or covered in a number of biocompatible compositions orpolymers, as known in the art.

FIGS. 2 and 3 depict two of the many optional embodiments of theflexible support member 3 and its optional coiled, ribbed, orinterlocking structure. The characteristics of this member can bedetermined by the desired flexibility, desired freedom of movement overa range of deflection angles, and/or desired strength or stress limitsor Young's modulus of the material and structure selected. As noted, anumber of polymeric, metal, and other material can be selected, and apreferred material is a shape-memory composition such as nitinol.Similarly and as noted above, the designs of FIGS. 10A-C can be used toproduce the interlocking structure of a flex support as shown in FIG. 2or 3, especially if laser cutting productions techniques are employed.

FIG. 4 depicts an embodiment with two pull wires 10 running through theflexible distal region assembly and the elements of the assembly. Whilepull wires 10 are shown to extend beyond anchor member or anchor ring 1,the pull wires can terminate at the holes or connection points in thering in optional embodiments. A central separating member 11 fits intoanchor member 1 in slits to effectively separate the interior of theflexible region so that pull wires 10 are held away from each other. Theflat, plate shape of separating member 11 is one embodiment, and severalother designs are possible especially when more than two pull wires areused. The separating member is typically a flexible element designed toflex and deflect with the assembly. The interlocking ribbed flex supportmember 12 adds structural stability and integrity to the assembly. Theflex support member 12 fits onto, inside, or is integrally formed intothe flexible region 3, which fits into the proximal end 1 of the shaft.The proximal end of the flexible region can also contain an anchormember or additional anchor member (not shown) to support or controlmovement of pull wires 10.

FIGS. 5 and 6 depict views of each side of the anchor member 1 and itsoptional features. Slots 21 are designed to hold or fix in a separatingposition the separating member 11, as shown in FIG. 4. Holes 23 aredesigned to allow pull wires to pass through and can be contoured to fita terminating ball or other fixed point at the end of a pull wire. Thediffering diameters shown on the profile of anchor member 1 allow forthe insertion into the flexible region of assembly. The anchor membercan optionally be placed at more than one position in a flexible regionassembly, such as at each of the proximal and distal end, and at thedistal end, the center or intermediate point of, and the proximal end ofthe flexible region.

FIG. 7 depicts a proximal end 13 connection point for the flexibleassembly, where slots 20 fix the separating member in position, andinserting diameter 16 region fits into the flexible region of assembly.FIGS. 8 and 9 depict the deflection of the flexible distal region to adesired angle.

The assemblies and devices of the invention can be used in methods toablate cardiac or epicardial tissue, or other tissue. The flexibleregion assembly can be designed to allow, for example, about 90 degreesof deflection, or from about 60 to about 100 degrees of deflection, to adistal end and maintain the integrity of the flexible region and controlover the movement of the ablating element at distal end. By maintainingthe integrity, the interior and/or exterior walls of the flexible regiondo not crimp, yield, crack, or break at maximum deflection.Alternatively, the interior and/or exterior walls can withstand multiplerounds of maximum deflection and release, such as 10 rounds, 20 rounds,or 50 rounds, without substantially effecting the integrity of theinterior or exterior walls by showing signs of crimping, cracking,yielding or breaking. Thus, for example, the pull wires can be actuatedat a handle at the proximal end of the device to fully deflect thedistal end to 90 degrees. The materials used in construction of theflexible region can be shape-memory materials that allow the flexibleregion to return to a desired position or move a desired angle to ablatetissue as controlled by pull wires. The deflection can be in one, two,or multiple directions with the use of a number of pull wires andconnection points of the pull wires to the device or within the flexibleregion. The angle of deflection in each direction desired, or range ofangles, can be selected from any number between, for example, 45 to 90degrees.

Although several embodiments of this invention have been described abovewith a certain degree of particularity, those skilled in the art couldmake numerous alterations to the disclosed embodiments without departingfrom the spirit or scope of this invention.

All directional references (e.g., upper, lower, upward, downward, left,right, leftward, rightward, top, bottom, above, below, vertical,horizontal, clockwise, and counterclockwise) are only used foridentification purposes to aid the reader's understanding of the presentinvention, and do not create limitations, particularly as to theposition, orientation, or use of the invention. Joinder references(e.g., attached, coupled, fixed, connected, and the like) are to beconstrued broadly and may include intermediate members between aconnection of elements and relative movement between elements. As such,joinder references do not necessarily infer that two elements aredirectly connected and in fixed relation to each other.

It is intended that all matter contained in the above description orshown in the accompanying drawings shall be interpreted as illustrativeonly and not limiting. Changes in detail or structure may be madewithout departing from the spirit of the invention as defined in theappended claims.

1. (canceled)
 2. A medical catheter component, comprising: a cylindricalbody including a circumferential wall defining an inner lumen; and aplurality of cuts through the circumferential wall of the cylindricalbody, wherein the plurality of cuts define a ribbed structure comprisinga first continuous spine extending from a first point on the cylindricalbody just proximal of a most proximal of the plurality of cuts to asecond point on the cylindrical body just distal of a most distal of theplurality of cuts.
 3. The medical device component according to claim 2,wherein the ribbed structure further comprises a second continuous spineextending from a third point on the cylindrical body just proximal ofthe most proximal of the plurality of cuts to a fourth point on thecylindrical body just distal of the most distal of the plurality ofcuts.
 4. The medical device component according to claim 2, wherein thesecond continuous spine is located diametrically opposite the firstcontinuous spine.
 5. The medical device component according to claim 2,wherein the first continuous spine has a switchback arrangement.
 6. Themedical device component according to claim 2, wherein the firstcontinuous spine comprises an uncut portion of the circumferential wallextending longitudinally along a length of the cylindrical body.
 7. Themedical device component according to claim 2, further comprising atri-lumenal insert positioned within the inner lumen of the cylindricalbody.
 8. The medical device component according to claim 7, wherein thetri-lumenal insert comprises an anchor member secured to a distalsection of the cylindrical body.
 9. The medical device componentaccording to claim 7, wherein the tri-lumenal insert comprises anhourglass-shaped central lumen and a pair of pull wire lumens positionedperipheral to the hourglass-shaped central lumen.
 10. The medical devicecomponent according to claim 9, wherein the pair of peripheral lumensare positioned opposite each other adjacent a neck of thehourglass-shaped central lumen.
 11. The medical device componentaccording to claim 2, wherein the cylindrical body comprises a shapememory material.
 12. A medical catheter component, comprising: acylindrical body including a wall that defines a plurality of lumens,the plurality of lumens comprising: an hourglass-shaped central lumen;and at least two additional lumens positioned peripheral of thehourglass-shaped central lumen.
 13. The medical device componentaccording to claim 12, wherein the at least two peripheral lumenscomprise a first peripheral lumen and a second peripheral lumen, andwherein the first and second peripheral lumens are positioned onopposite sides of a neck of the hourglass-shaped central lumen.
 14. Amedical catheter, comprising: a cylindrical body including a pluralityof lumens, the plurality of lumens comprising: an hourglass-shapedcentral lumen including a central portion and a peripheral portion; andat least two peripheral lumens each configured to slidably receive apull wire therein, wherein the at least two peripheral lumens are eachcoextensive with the peripheral portion of the hourglass-shaped centrallumen.
 15. The medical catheter according to claim 14, wherein the atleast two peripheral lumens comprise a first peripheral lumen and asecond peripheral lumen, and wherein the first and second peripherallumens are positioned on opposite sides of a neck of thehourglass-shaped central lumen.
 16. The medical catheter according toclaim 14, wherein the cylindrical body comprises a plurality of cutsthrough a circumferential wall of the cylindrical body, the plurality ofcuts defining a ribbed structure comprising a first continuous spineextending from a first point on the cylindrical body just proximal of amost proximal of the plurality of cuts to a second point on thecylindrical body just distal of a most distal of the plurality of cuts.17. The medical catheter according to claim 16, wherein the ribbedstructure further comprises a second continuous spine extending from athird point on the cylindrical body just proximal of the most proximalof the plurality of cuts to a fourth point on the cylindrical body justdistal of the most distal of the plurality of cuts.
 18. The medicalcatheter according to claim 17, wherein the second continuous spine islocated diametrically opposite the first continuous spine.
 19. Themedical catheter according to claim 17, wherein the first continuousspine has a switchback arrangement.
 20. The medical catheter accordingto claim 16, wherein the first continuous spine comprises an uncutportion of the circumferential wall extending longitudinally along alength of the cylindrical body.
 21. The medical catheter according toclaim 14, wherein the cylindrical body comprises a shape memorymaterial.